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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1865859생성일: 2026년 10월 26일

Dimethylformamide → (S)-2-(4'-Cyclopropylcarbamoyl-biphenyl-3-ylcarbamoyl)-pyrrolidine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/1865859

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물4-bromo-N-cyclopropylbenzamideHCID 882949—
반응물(S)-2-[3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenylcarbamoyl]-pyrrolidine-1-carboxylic acid benzyl esterHCID 24828649—
용매MethanolHCID 887—
용매Sodium BicarbonateHCID 516892—
생성물(S)-2-(4'-Cyclopropylcarbamoyl-biphenyl-3-ylcarbamoyl)-pyrrolidine-1-carboxylic acid benzyl esterHCID 57977817—

반응 조건

온도70 °C

반응 단계

A solution of (S)-2-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenylcarbamoyl]-pyrrolidine-1-carboxylic acid benzyl ester (74 mg, 0.16 mmol), 4-bromo-N-cyclopropyl-benzamide (39.7 mg, 0.17 mmol), and Pd[P(Ph)3]4 (13.7 mg, 7.2 mol %) in methanol (2 mL), NaHCO3 (sat. aq., 300 μL), and DMF (400 μL) was degassed and heated to 70° C. overnight in a sealed vial. The reaction was cooled, filtered, and purified by reverse phase HPLC to give the desired product. Yield 5.3 mg. MS: 484.2 (M+H+); H1 NMR (DMSO-d6): δ (ppm) 0.51-0.70 (m, 4H), 1.76-1.98 (m, 3H), 2.08-2.30 (m, 1H), 2.77-2.86 (m, 1H), 3.38-3.52 (m, 2H), 4.27-4.37 (m, 1H), 4.86-5.08 (m, 2H), 6.96-7.65 (m, 7

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07629340B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-e0e286ce79ba47c39297daa10c5b9eea
출처 메모uspto-grants-2009_12